Canonical Allele Identifier: CA371940696

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 1429169
• ClinVar RCV Id: RCV001938796
• dbSNP Id: rs2131136061
• MyVariant Identifiers: chr8:g.106801006T>C (hg19) ; chr8:g.105788778T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105788778T>C , CM000670.2:g.105788778T>C	GRCh38
NC_000008.10:g.106801006T>C , CM000670.1:g.106801006T>C	GRCh37
NC_000008.9:g.106870182T>C	NCBI36
NG_011723.1:g.474860T>C
NG_011723.2:g.474860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.593T>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Phe198Ser
ENST00000407775.6:c.593T>C (ZFPM2)	ENSP00000384179.2:p.Phe198Ser
ENST00000511341.6:n.1333T>C (ZFPM2)
ENST00000517361.1:c.197T>C (ZFPM2)	ENSP00000428720.1:p.Phe66Ser
ENST00000520492.5:c.197T>C (ZFPM2)	ENSP00000430757.1:p.Phe66Ser
ENST00000522296.1:n.107T>C (ZFPM2)
NM_012082.3:c.593T>C (ZFPM2)	NP_036214.2:p.Phe198Ser
NR_125796.1:n.298-1182A>G (ZFPM2-AS1)
NR_125797.1:n.309-6295A>G (ZFPM2-AS1)
XM_011516946.1:c.632T>C (ZFPM2)	XP_011515248.1:p.Phe211Ser
XM_011516947.1:c.563T>C (ZFPM2)	XP_011515249.1:p.Phe188Ser
XM_011516948.1:c.434T>C (ZFPM2)	XP_011515250.1:p.Phe145Ser
XM_011516949.1:c.572-9946T>C (ZFPM2)	XP_011515251.1:n.572-9946T>C
NM_001362836.1:c.434T>C (ZFPM2)	NP_001349765.1:p.Phe145Ser
NM_001362837.1:c.197T>C (ZFPM2)	NP_001349766.1:p.Phe66Ser
XM_011516947.3:c.563T>C (ZFPM2)	XP_011515249.1:p.Phe188Ser
NM_012082.4:c.593T>C (ZFPM2) MANE Select	NP_036214.2:p.Phe198Ser
NM_001362836.2:c.434T>C (ZFPM2)	NP_001349765.1:p.Phe145Ser
NM_001362837.2:c.197T>C (ZFPM2)	NP_001349766.1:p.Phe66Ser